Pascal Medical AB
Country not established
- Devices
- 1
What Pascal Medical AB makes
Pascal Medical AB manufactures the PASCAL MEDICAL AB MENIETT 20, a device designed for minimally invasive spinal procedures, including vertebroplasty and kyphoplasty.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device. The device is listed in the US regulatory registry.
Catalogue
Pascal Medical Ab Meniett 20 Ref K991562
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pascal Medical AB have in the registry?
The registry currently lists 1 device for Pascal Medical AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pascal Medical AB's devices?
Among its 1 most recently registered device, Pascal Medical AB has devices listed in FDA 510(k) (1 device).
What risk classes do Pascal Medical AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pascal Medical AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pascal Medical AB in the registry?
The most recently registered devices listed for Pascal Medical AB include PASCAL MEDICAL AB MENIETT 20.